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pubmed-article:15479735pubmed:abstractTextTalin, an adaptor between integrin and the actin cytoskeleton at sites of cell adhesion, was recently found to be present at neuronal synapses, where its function remains unknown. Talin interacts with phosphatidylinositol-(4)-phosphate 5-kinase type Igamma, the major phosphatidylinositol-(4,5)-bisphosphate [PI(4,5)P(2)]-synthesizing enzyme in brain. To gain insight into the synaptic role of talin, we microinjected into the large lamprey axons reagents that compete the talin-PIP kinase interaction and then examined their effects on synaptic structure. A dramatic decrease of synaptic actin and an impairment of clathrin-mediated synaptic vesicle endocytosis were observed. The endocytic defect included an accumulation of clathrin-coated pits with wide necks, as previously observed after perturbing actin at these synapses. Thus, the interaction of PIP kinase with talin in presynaptic compartments provides a mechanism to coordinate PI(4,5)P(2) synthesis, actin dynamics, and endocytosis, and further supports a functional link between actin and clathrin-mediated endocytosis.lld:pubmed
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pubmed-article:15479735pubmed:articleTitleA role for talin in presynaptic function.lld:pubmed
pubmed-article:15479735pubmed:affiliationDepartment of Cell Biology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06519, USA.lld:pubmed
pubmed-article:15479735pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15479735pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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